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A mutation linked to retinitis pigmentosa in HPRP31 causes protein instability and impairs its interactions with spliceosomal snRNPs
- 1.0334100 - ÚMG 2010 RIV GB eng J - Journal Article
Huranová, Martina - Hnilicová, Jarmila - Fleischer, Branislav - Cvačková, Zuzana - Staněk, David
A mutation linked to retinitis pigmentosa in HPRP31 causes protein instability and impairs its interactions with spliceosomal snRNPs.
Human Molecular Genetics. Roč. 18, č. 11 (2009), s. 2014-2023. ISSN 0964-6906. E-ISSN 1460-2083
R&D Projects: GA AV ČR KAN200520801
Grant - others:Max Planck Society(DE) Partner group program
Institutional research plan: CEZ:AV0Z50520514
Keywords : retinitis pigmentosa * snRNP * splicing
Subject RIV: EB - Genetics ; Molecular Biology
Impact factor: 7.386, year: 2009
Permanent Link: http://hdl.handle.net/11104/0178923
Number of the records: 1